Tetrachlorophthalic acid Chemical Properties

Melting point:

98°C

Boiling point:

418.21°C (rough estimate)

Density 

1.8331 (rough estimate)

refractive index 

1.5282 (estimate)

storage temp. 

Sealed in dry,Room Temperature

solubility 

soluble in Methanol

form 

powder to crystal

pka

0.55±0.32(Predicted)

color 

White

Water Solubility 

Sparingly soluble

Stability:

Stable. Incompatible with strong oxidizing agents.

CAS DataBase Reference

632-58-6(CAS DataBase Reference)

EPA Substance Registry System

Tetrachlorophthalic acid (632-58-6)

Safety Information

Risk Statements 

36/37/38

Safety Statements 

36/37/39

RTECS 

TI2795000

HS Code 

2917.39.7000

MSDS

• Language:English Provider:Tetrachlorophthalic acid

Tetrachlorophthalic acid Usage And Synthesis

Chemical Properties

colourless crystals

Uses

Dyes, intermediates.

General Description

Colorless plates.

Air & Water Reactions

Sparingly water soluble.

Reactivity Profile

A chlorinated organic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Tetrachlorophthalic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.

Fire Hazard

Flash point data for Tetrachlorophthalic acid are not available; Tetrachlorophthalic acid is probably combustible.

Tetrachlorophthalic acid (632-58-6)Related Product Information

• Citric acid
• Dimethyl phthalate
• 3-Chloroperoxybenzoic acid
• Potassium hydrogen phthalate
• 2-Iodobenzoic acid
• Diisobutyl phthalate
• Ethyl 2-(Chlorosulfonyl)acetate
• Bis(2-ethylhexyl) phthalate
• Dibutyl phthalate
• Diethyl phthalate
• Phthalic acid
• Hyaluronic acid
• Methyl anthranilate
• Folic acid
• Ascoric Acid
• Anthranilic acid
• DI-N-BUTYL TETRACHLOROPHTHALATE
• 3,4,5,6-Tetrachlorophthalic Acid